Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  7
• Reference
  J:41347 Cattanach BM, et al., A candidate model for Angelman syndrome in the mouse. Mamm Genome. 1997 Jul;8(7):472-8
• ID
  MGI:1096451

Genes

Gene	Assay Type
Oca2	visible phenotype
Snrpn	PCR amplified length variant
D7Hms1	other
Mkrn3	reported elsewhere
T(7;15)9H	visible phenotype
Igf2	other

Notes

• Reference
  Authors use Dn34 for locus symbol D7Hms1.
• Experiment
  A region of mouse Chromosome 7 that exhibits maternal (MatDup. Prox 7) and paternal duplication (PatDup. Prox 7) is considered as a model for Anglman syndrome (AS). Analysis using various translocation stocks was informative to show the following order of loci within this region. IsCt - p - Snrpn - D7Hms1 - Mkrn3 - T(7;15)9H - Igf2, where IsCt is an insertional translocation.